Variant #0000259405 (NC_000009.11:g.136433778G>A, NM_001145320.1:c.2142G>A (ADAMTSL2))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.136433778G>A
DNA change (hg38) g.133568656G>A
Published as ADAMTSL2(NM_001145320.2):c.2142G>A (p.S714=)
ISCN -
DB-ID ADAMTSL2_000059 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAMTSL2 NM_001145320.1 -?/. - c.2142G>A r.(?) p.(Ser714=)
ADAMTSL2 NM_014694.3 -?/. - c.2142G>A r.(?) p.(Ser714=)


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